IT WAS ALWAYS A FAKE VACCINE

They were never vaccines to begin with. It was always a lie from the beginning.  

Dr. Ryan Cole: 15 Ways the COVID Shots Injure and KiII

According to Dr. Ryan Cole, the COVID shots can cause harm in 15 distinct ways. Researchers have revealed how nanoparticles are being utilized in these shots, and what the effects are of the persistence of synthetic RNA in the body. Additionally, scientists are exposing the circulation of synthetic spike protein and its impact on human health. The spike protein itself is a harmful agent that can have far-reaching consequences. Experts are also examining the brain accumulation and impact of these shots, as well as the potential for peripheral nerve damage and organ damage. Furthermore, the COVID shots have been linked to myocarditis and heart issues, and are also affecting the adrenal glands and elastic fibers. The shots are also causing reproductive harms, weakening immune systems, and leading to vascular damage and clotting. Moreover, abnormal protein accumulation, immune tolerance, and increased cancer risk are all being actively studied as potential consequences of the COVID shots. Dr. Cole’s insights highlight the need for continued research into the effects of these shots on human health and the need to stop them.

Vaccine injections altered human immunity on a global scale

According to epidemiologist Nicolas Hulscher, vaccine injections have drastically changed human immunity worldwide, and he’s sounding the alarm. By analyzing the electronic medical records of thousands of patients before and after the COVID-19 pandemic, Hulscher has uncovered compelling evidence of vaccine-acquired immunodeficiency syndrome, or VAIDS. The shocking spike in autoimmune diseases, chronic infections, and even cancer cases is prompting Hulscher to call for immediate and thorough scientific scrutiny of the long-term consequences of these vaccines, with the ultimate goal of potentially bringing an end to the mRNA vaccine era. Hulscher’s findings are sparking intense debate and raising critical questions about the safety and efficacy of these vaccines, and he’s urging the scientific community to take a closer look at the devastating impact they may be having on human health.

 mRNA tech is NOT a vaccine — it’s an experimental gene-modifying platform

Under oath, Dr. Robert Sullivan confirmed it. mRNA tech is NOT a vaccine — it’s an experimental gene-modifying platform. It forces the body to produce toxic spike proteins, causing lung, heart, and organ damage. It is linked to autoimmune disorders and abnormal cell growth, and they KNEW IT. These are crimes against humanity were committed, the truth was censored to protect Big Pharma and billions were made — at the cost of YOUR health

What is Gene Therapy, and Why the Interest?

Gene therapy involves modifying or introducing genetic material to treat or prevent diseases, often targeting conditions like genetic disorders, cancers, or viral infections. It’s a broad field, encompassing mRNA vaccines (which some call gene therapy due to their use of genetic instructions) and approaches like CRISPR or viral vector therapies. According to dubious researchers and institutions, it offers potential cures for previously untreatable conditions, rapid vaccine development (as seen with COVID-19), and massive commercial opportunities. Biotech giants like Moderna and Pfizer, backed by government contracts, have poured billions into this space, with mRNA platforms alone generating tens of billions in revenue during the pandemic.

mRNA is about Centralized Control and Power

The push for gene therapy is tied to powerful institutions—Big Pharma, governments, and organizations like the World Health Organization or the Gates Foundation—that are centralizing control over health. Globalist entities—think WHO, GAVI, or multinational corporations—are accused of using gene therapy to standardize medical interventions worldwide, bypassing national sovereignty. mRNA vaccines, rolled out globally during COVID-19, were a test case for mandating experimental tech under the guise of public health. gene therapies could be weaponized to alter populations, either through sterilization, genetic selection, or other dystopian outcomes, echoing historical eugenics programs.

Eugenics, as practiced in the early 20th century, involved elites promoting policies to “improve” populations, often targeting marginalized groups. Figures like Bill Gates, whose foundation funds vaccine and gene therapy research, has made comments on population control through health interventions. While Gates frames this as reducing poverty to lower birth rates, its a slippery slope toward eugenics-like goals, especially when gene-editing tools like CRISPR could target specific genetic traits.

mRNA is a Trojan Horse

mRNA vaccines as “gene therapy” because they introduce genetic instructions into cells. They’re a gateway to normalizing genetic manipulation. Kennedy’s recent cancellation of $500 million in mRNA funding cited safety, resonating with those who see mRNA as a tool for globalist agendas rather than public good.

mRNA for Profit and Power Concentration

From a finance angle, gene therapy is a goldmine. The global market is projected to hit $13 billion by 2026, driven by high-cost treatments (some therapies cost $2M+ per dose). This enriches a small elite—pharma CEOs, investors, and their political allies—while tying healthcare to corporate control. The gene therapy’s push isn’t just about health but about creating dependency on proprietary tech, with potential for social engineering if access is gatekept or tailored to certain groups.

Written By Tatenda Belle Panashe

PETER MARKS & THE FDA’S COVER-UP OF THE HARMS OF COVID JABS

Now, proceeding to look further into Peter Marks’ works at the FDA, many have been horrified to learn that the FDA and CDC systematically ignored every possible sign the COVID vaccines were dangerous as they pushed it on more and more people. One of the ways people were made aware of this was through the recently leaked recordings showing how stubbornly the head of FDA’s vaccine division, being Peter Marks at the time, refused to acknowledge any of the evidence brought forward by a group of permanently injured vaccine recipients, and even medical practitioners who were treating vaccine injured patients.

Here’s why this is important to note: generally, in looking through what transpired with the COVID-19 response, Anthony Fauci is commonly blamed for all that went amiss – and correctly so. However, we must not also miss the people who were also directly involved, while hidden within the FDA bureaucracy; and one such person is Peter Marks. Peter Marks is the primary person who covered up the reports of COVID vaccine injuries (and instead repeatedly told the world they were (quote unquote) “safe and effective”).

He was also the person who kept on pushing the FDA’s chief vaccine scientists (who were very pro-vaccine) to accelerate and condense the approval timelines for the COVID jabs (as those approvals were needed to legally implement Biden’s vaccine and booster mandates). The parties involved in this process, which included, Marion Gruber and Philip Krause (who were the Director and Deputy Director of the FDA’s Office of Vaccines Research and Review, respectively); they reported that there were (at that point) no more corners they could cut to further accelerate the COVID vaccine approvals, at which point they were removed from the COVID vaccine approval process and Peter Marks took it over (at which point the unjustifiable approvals and mandates quickly followed).

BUT, despite all of this, the media lied about Peter Marks. They stated that Marks was pressured to be anti-vax by RFK Jr. Yet, no single specific action is cited. Some articles even call Marks a hero, and he is praised by past FDA officials who now consult for drug companies or serve on their board. And funny enough, Peter Marks has now joined their ranks as one among those who embody the problem with the revolving- door corruption between the FDA and the corporations it is supposed to regulate – especially pharmaceutical companies.

FROM FDA REGULATOR TO ELI LILLY EXECUTIVE — THE REVOLVING DOOR OF CORRUPTION EXPANDS

More specifically, six months after his removal from the FDA’s Center for Biologics Evaluation and Research (CBER), Peter Marks has officially joined Eli Lilly — the same company that has become notorious for particularly employing former FDA officials. In any case, Marks will serve as Senior VP for Molecule Discovery and Head of Infectious Diseases, working alongside Rachael Anatol, who is another recently ousted regulator. Meanwhile, his former FDA counterpart Patrizia Cavazzoni also quietly landed at Pfizer as Chief Medical Officer earlier this year.

IN FACT, nine of the last ten FDA commissioners have actually gone on to work for major pharmaceutical companies shortly after leaving public office. Within the Bio-Pharmaceutical Complex, officials routinely rotate between government agencies, global NGOs, and Big Pharma — advancing personal careers while deepening institutional entanglements across the syndicate. And to paint a picture of both this corrupt revolving door relationship and also just how global this syndicate is.

Dr Elizabeth Nabel, who is the former Director of the National Heart, Lung, and Blood Institute (NHLBI) at the NIH — Joined Moderna’s Board of Directors. Dr Scott Gottlieb, who is the former FDA Commissioner — Joined the Board of Pfizer to promote vaccines on TV during pandemic. Dr Stephen Hahn, the former FDA Commissioner — Became Chief Medical Officer at Flagship Pioneering, which is the venture capital firm that launched Moderna. Sir Jonathan Van-Tam, who is the United Kingdom’s former Deputy Chief Medical Officer and member of the Vaccine Task Force — he was appointed as Senior Medical Consultant at Moderna. Then, Dr Jeremy Farrar, the former Director of the Wellcome Trust — he was appointed as Chief Scientist at the World Health Organization (WHO).

In addition, Dr Soren Brostrom, the Director General of the Danish Health Authority — he was also elected to the Executive Board of the World Health Organization. Then, Dr Moncef Slaoui, who is the former Chief Scientist of Operation Warp Speed — he previously served as an executive at GlaxoSmithKline (GSK) and as a Board member at Moderna. Dr Julie Gerberding, who is the former CDC Director — became President of Merck Vaccines, later serving as CEO of the Foundation for the National Institutes of Health (the NIH). There is also Dr Luciana Borio, the former FDA Acting Chief Scientist and member of the Biden COVID-19 Advisory Board — she became a Partner at ARCH Venture Partners, which is a firm heavily invested in biotech, while (as we just alluded) Dr Patrizia Cavazzoni, the former Director of the FDA’s Center for Drug Evaluation and Research (CDER) — Appointed as Chief Medical Officer at Pfizer, and Dr Peter Marks, the former Director of the FDA’s Center for Biologics Evaluation and Research (CBER) — has recently been appointed Senior Vice President for Molecule Discovery and Head of Infectious Diseases at Eli Lilly.

It is jarring how repetitive and global this revolving door corruption is; it is factually a syndicate that has gotten so bold in its endeavours, that it has become a network that erases the line between public health stewardship and corporate profiteering — which is a deeply embedded conflict of interest that undermines both trust and safety.

THE REVOLVING DOOR CORRUPTION IS INDICATIVE OF A BROADER ISSUE OF DIABOLICAL CORPORATIONS

Now here is why this revolving door issue matters beyond the specific individuals who are involved in it. A frequent criticism of corporations (which I believe also applies to governmental bureaucracies) is that their organisational structure encourages sociopathic behaviour – in fact, you would have heard me quote the President of Loveworld Incorporated, the highly esteemed Rev Dr Chris Oyakhilome DSc DSc DD, when he warned that “Capitalism has metamorphosed”, in that while we used to have corporations that sought to make profit through contributing products and services that added a net positive to society, that has since changed for a handful of them, and now they seek to make profit at the expense of the best interest of society.

Well, this typically occurs because MEMBERS of these entities are shielded from legal or personal accountability for their actions, with any wrongdoings being attributed to the corporation as a whole. In contrast, the main form of accountability most members face is the pressure to advance the institution’s mission (e.g., to make more money), leading to the proliferation of increasingly unethical methods to achieve that goal. To illustrate this, consider this quote from Peter Rost, who is a former executive at Pfizer and one of the few pharmaceutical leaders to speak out against the industry: He stated that (quote):

“It is scary how many similarities there are between this industry [speaking about the pharmaceutical industry] and the mob. The mob makes obscene amounts of money, as does this industry. The side effects of organised crime are killings and deaths, and the side effects are the same in this industry. The mob bribes politicians and others, and so does the drug industry … The difference is, all these people in the drug industry look upon themselves – well, I’d say 99 percent, anyway – look upon themselves as law-abiding citizens, not as citizens who would ever rob a bank … However, when they get together as a group and manage these corporations, something seems to happen … to otherwise good citizens when they are part of a corporation. It’s almost like when you have war atrocities; people do things they don’t think they’re capable of. When you’re in a group, people can do things they otherwise wouldn’t, because the group can validate what you’re doing as okay.”

Now, this genuinely sounds like a cry for help, from someone who fell into the pharmaceutical rabbit hole, only to discover later that they had become everything that they found morally reprehensible. Which clarifies, in part, how many of the people in this industry overlook what they know and are asked to do. But, on the other hand, we also know that there are those who are driven by their gain: be it power brockering or money. For instance, during the COVID plandemic, there was essentially zero daylight between Anthony Fauci’s agencies and the pharmaceutical industry; and this incestuous relationship was a significant part of the problem. But, here’s more on the propensity of pharmaceutical companies to function like the mafia or mob.

Furthermore, why this revolving door issue matters beyond the specific individuals who are involved in it is that it also points to a culture of disregard for morally acceptable or ethical conduct. In other words, pharmaceutical companies had a streak where they just did not fear consequences as much as they should, because they often got away with very heinous conduct – either through out-of-court settlements, or because of the work done through the pharmaceutical lobby. As such, this created a culture of outright corruption.

For instance, you’d recall that in May this year, the FDA Commissioner in this second Trump administration, being Dr Martin Makary, he publicly exposed a longstanding practice where agency inspectors accepted luxury limousine rides from the very pharmaceutical corporations they were tasked with overseeing. This underscores deep-seated conflicts of interest that have undermined the integrity of drug safety inspections, especially at overseas manufacturing facilities.

Now, the issue centers on foreign inspections, where the FDA’s oversight of drug production has historically relied on “scheduled” visits—essentially announced in advance. These setups, Makary argues, are “no inspections at all. They’re a joke.” Companies get ample time to polish their operations, hide violations, and even roll out the red carpet. Enter the limos: lavish rides provided by inspected firms, blurring the line between regulator and regulatee. While not outright bribes, such perks create an aura of favoritism, potentially softening enforcement. Makary’s exposure highlights how these rides were routine, eroding public trust in the FDA’s gold-standard claims. And this is not hyperbole; especially as the numbers paint a grim picture.

In particular, the FDA inspects thousands of foreign facilities annually, many in countries like India and China, which produce up to 80% of active pharmaceutical ingredients for U.S. drugs. A 2023 Government Accountability Office report flagged delays and weaknesses in these checks, exacerbated by COVID-19 travel bans. But post-pandemic, the return to fieldwork revealed these ethical lapses. In response, the FDA announced an expansion of unannounced inspections in May 2025, aiming to catch bad actors off-guard—those falsifying records or concealing contamination risks. The policy also explicitly bans inspectors from accepting industry-provided transport, including taxis, limos, or for-hire vehicles, alongside lodging perks. “This is a key step… to ensure that the FDA is the gold standard for regulatory oversight,

WORLD’S FIRST INTERNATIONAL GOVERNING BODY DECLARES mRNA INJECTIONS BIOLOGICAL & TECHNOLOGICAL WMDS

But, while all of this happens, there are strong efforts that are pushing against the works of pharmaceutical companies, and the vaccine holocaust. Notable among them is that in a stunning and historic move, the Alliance of Indigenous Nations (or A.I.N.) International Tribunal has issued an ORDER and DECLARATION stating that “mRNA nanoparticle injections are in fact biological and technological weapons of mass destruction.” And, of course, this marks the first formal judicial declaration by any recognized international authority categorizing the COVID-19 mRNA products as biological weapons.

Now, also important to note is that, in December 2024, Canada’s Ministry of Crown–Indigenous Relations and Northern Affairs (CIRNAC) formally acknowledged the Alliance of Indigenous Nations, its Treaty, and its International Tribunal—a judicial body composed of judges from every continent. In its official letter dated December 13, 2024, Canada affirmed that its relationship with the A.I.N. exists on a Nation-to-Nation basis, thereby recognizing the Tribunal as a sovereign legal authority under Indigenous and international law.

Also important to note is that the declaration by the Alliance of Indigenous Nations International Tribunal that the COVID vaccine is a biological and technological weapons of mass destruction aligns with our recent study by Zywiec et al, which demonstrated that the COVID-19 mRNA injections violate the Biological Weapons Convention, the Nuremberg Code, the Helsinki Declaration, and the US Constitution. It also aligns with Minnesota Bill HF3219, which classifies mRNA injections and related products as weapons of mass destruction under Section 609.712, prohibiting their possession or distribution within the state.

Written By Lindokuhle Mabaso

Healthcare as one of the 7 areas that globalists seek to manipulate, and we ought to start with some historical context, regarding how the COVID plandemic enabled globalists to test a militarised healthcare system.

Now, in former US president Eisenhower’s farewell speech of January 17, 1961, he stated that “…in the councils of government, we must guard against the acquisition of unwarranted influence, whether sought or unsought, by the military-industrial complex.” Sixty-three years on, many understand what he was referring to. We’ve seen the cycle of undeclared wars and decades-long foreign occupations that are undertaken on nebulous or even outright false pretences. We’ve also seen the ever-hungry mega-industry that produces super-expensive, high-tech killing devices of every imaginable form, as well as the steady stream of traumatised soldiers that it spits out. Evidently, war, to some, has become big business! And as Eisenhower warned, as long as those profiting from it drive the policy and the money stream (in other words – if they can weaponise the laws), the MIC will continue to grow.

In light of this contextualisation of the MIC, one would think that other mega-industries – the medical industry in particular – have generally fared better in public perception than the military-industrial complex; in that this MIC seemed a far more diabolical industry. Well, that was until the covid pandemic, but not forsaking a number of prior controversies. But this is really to say that among its many lessons, the Covid plandemic era has taught us this: if you substitute Pfizer and Moderna for Raytheon and Lockheed Martin, and swap the NIH and CDC for the Pentagon, you essentially get the same result. Meaning that not only is the “medical-industrial complex” every bit as real as its military-industrial counterpart, but, it is also every bit as real a problem, precisely because they are different sides of the same coin since the military industrial complex informed the weaponisation of the healthcare system in the COVID era. So, how did this happen?

Well, during the Covid era, one can infer interesting parallels to military operations. For instance, by early-to-mid 2020, it became obvious to those paying attention that the Covid “response,” while promoted as a medical initiative, was in fact a military operation. Martial law had effectively been declared in March 2020, after the Covid response (and practically speaking, control of the nation) was ceded to the National Security Council. Civil liberties – including the freedoms of assembly, worship, the right to travel, to earn one’s living, to pursue one’s education, or to obtain legal relief – were rendered null and void. In addition, top-down diktats on how to manage Covid patients were handed down to physicians from high above, and these were enforced with a militaristic rigidity unseen in doctors’ professional lifetimes. Meanwhile, the mandated protocols also made no sense: they ignored fundamental tenets of both sound medical practice and medical ethics; they shamelessly lied about well-known interventions, while their mandated protocols killed people.

What was also interesting to note during that time is that those physicians and other professionals who spoke out were effectively court-martialed. State medical boards, specialty certification boards, and large healthcare system employers virtually tripped over each other in the rush to de-license, decertify, and fire dissenters. Genuine, courageous physicians who actually treat patients, such as Peter McCullough, Mary Talley Bowden, Scott Jensen, Simone Gold, and others, were persecuted, while non-practicing bureaucrats like Anthony Fauci were hailed with false titles like “America’s Top Doctor.” The propaganda was as nauseating as it was blatant. And the subsequent violence was no different.

But, speaking of lies about well-known interventions, you’d recall the ivermectin debate, that president Trump was involved in during that period. Well, as more evidence came out supporting Trump’s claim of the comparative benefit of using ivermectin in comparison to vaccines and all other protocols that were mandated, the FDA in the Biden era, even tried to back-peddle on their dismissal of ivermectin. In particular, the FDA claimed their Ivermectin smear campaign was only related to people self-medicating w/ a veterinary formulation of the drug.

However, in a 2021 interview with the American Medical Association, FDA Director John Farley discouraged physicians from prescribing Ivermectin, calling it a ‘tragic choice’. He stated that (quote): “Making that choice to choose Ivermectin over a vaccine can be a tragic choice that can lead to them getting very sick, getting admitted to the hospital, or even dying from COVID.

This ultimately means that the concerning tenets that have driven the military industrial complex were incorporated into the healthcare system. During covid, globalist debuted this militarised so-called healthcare response, and thus in seeking to manipulate healthcare, want similar control. Why else would there be a WHO pandemic treaty and IHR that try to centralise power to dictate health policy on the Director General, except to great a legal justification for a militarised top down approach to global healthcare?

MEDICINE BECAME BIG BUSINESS: THE COMMERCIALISATION OF SICKNESS AND INFIRMITY 

Now, in light of the parallels between the military and the medical industrial complexes, we alluded to the fact that in light of the operations of the military industrial complex, war has become big business. Well, as far as institutional capture is concerned, the medical establishment has done the same, especially with cancer. You’d recall that we discussed here on ‘The War Room’ how not only is cancer man-made, but it is also big business, a multi-billion dollar industry. It involves getting people to get cancer, to be poisoned with chemotherapy, and large amounts of money spent on continuous research for a cure that apparently does not exist (which is a lie). And the biggest proof of this intentional weaponisation and commercialisation of cancer is that, simply put, cancer did NOT really exist more than 50 years ago but started booming with the introduction of processed food loaded with massive amounts of sugar and chemicals.

So, you’ve just heard the President of Loveworld Incorporated, the highly esteemed Rev. Dr Chris Oyakhilome DSc. DSc. DD. warn about the artificial and genetically modified food that causes cancer. Well, another crucial cause is exposure to carcinogenic systems. Now, a carcinogen is any substance, agent, or process that can induce cancer. They can cause cancer by damaging DNA or interfering with cellular processes (hence cancer is known as an attack on healthy cells by a cancerous cell). Examples of these carcinogens include asbestos, benzene, radon and even tobacco smoke.

This is critical to note because it exposes a detrimental irony when it comes to chemotherapy. Chemotherapy is also a carcinogenic system! It is inherently a harmful concoction of chemicals that was initially created as a weapon, and then suddenly became rebranded as a highly profitable health intervention.

There you have it, this same chemical agent that was used to kill people is now being used to allegedly treat cancer. And ironically, despite the modifications on it, chemotherapy can also function as a carcinogen! More specifically, chemotherapy drugs are designed to target and destroy rapidly dividing cells, including cancer cells, but they can also affect healthy cells that divide quickly, like those in the bone marrow, hair follicles, and digestive tract. However, some chemotherapy agents, particularly alkylating agents, have been linked to an increased risk of developing certain types of leukemia or other secondary cancers. And the risk of developing a second cancer after chemotherapy is influenced by factors like the type of chemotherapy drugs used, the dosage, the duration of treatment, and the individual’s overall health. ALL of this is to say that (IRONICALLY) chemotherapy also functions as a carcinogen, meaning that it is a cancer causing agent.

And so this details the institutionalisation of the commercialisation of sickness and infirmity. The medical industrial complex sees sickness as an opportunity to form a market or customer base; and so, this industry interventions that it knows are harmful or not effective in the long run, and merely brands them as an acceptable panacea. What makes this a problem of institutional corruption, as opposed to mere isolated cases of unethical business conduct is that this is standard practice in the medical industry – all while legitimate or just better cures are hidden.

Take Dr Patrick Soon-Shiong, who we recently discussed. So, in an interview with Tucker Carlson he detailed that there actually is a medical breakthrough in fighting cancer. However, because of politics, the Deep State and Big Pharma it’s being suppressed. Meaning that there is an intervention for which he has the data and research to prove has been helpful, yet special interests block it – pointing to systemic institutional corruption in the medical industry. Meanwhile, Dr Mark Hyman also told Tucker Carlson about the keto diet’s ability to fight cancer, diabetes, Alzheimer’s, schizophrenia and more. And so, literally eating certain good organic foods, is a comparatively far better option to chemotherapy.

MEDICAL ASSOCIATIONS: THE MEDICAL CARTEL’S TOOL FOR WEAPONISING LAWS

We then also have to address how the medical industrial complex weaponised laws, through formal legal avenues and also through the establishment of organisations that serve special interests. For instance, we’ve spoken about the audacious incident where the American Academy of Pediatrics, American College of Physicians, the American Public Health Association, and the Infectious Diseases Society of America have filed a federal lawsuit against Health Secretary Robert F. Kennedy Jr for withdrawing COVID-19 vaccine recommendations for healthy children and pregnant women.

The cartel also demanded a federal judge reinstate the COVID shot recommendations (again for children and pregnant women)—and block the US Department of HHS from enforcing or promoting RFK Jr’s May directive that removed them. Then, they also argued that Kennedy’s directive violates (quote) “norms” by bypassing the CDC and its ACIP panel, and undermines their ability to push the shot to patients and secure insurance coverage. This revealed a jarring display of the audacity of the medical industrial complex to use laws to fight or undermine progress. Because they obviously know that there are serious ramifications from the COVID jabs, but were adamant to use formal legal structures to block the US Department of HHS from enforcing or promoting RFK Jr’s May directive that removed those jabs from the recommendation list.

Similarly, we’ve been told to “listen to scientists” for years, while their credibility was tied to medical societies and associations that vouched for their alleged credibility. BUT… the dark and corrupt history behind the largest group of health professionals in the US, being the American Medical Association, suggests that these organisations are part of the problem of systemic institutional rot and corruption.

Thankfully, the corruption of these medical associations is being exposed on the regular today. For example, files from the World Professional Association for Transgender Health (also called WPATH) prove that the practice of transgender medicine is neither scientific nor medical. The American Medical Association, The Endocrine Society, the American Academy of Pediatrics, and thousands of doctors worldwide rely on WPATH. It is considered the leading global authority on gender medicine.

And yet WPATH’s internal files, which include written discussions and a video, reveal that its members know they are creating victims and not getting “informed consent.” Victims include a 10-year-old girl, a 13-year-old developmentally delayed adolescent, and individuals suffering from schizophrenia and other serious mental illnesses. Meanwhile, WPATH members indicate repeatedly that they know that many children and their parents don’t understand the effects that puberty blockers, hormones, and surgeries will have on their bodies. And yet, they continue to perform and advocate for gender medicine. In any case, the WPATH Files prove that gender medicine is comprised of unregulated and pseudoscientific experiments on children, adolescents, and vulnerable adults.

Then there is also the American Heart Association. This association exposes systemic corruption in the medical industry in that it also serves to propagate false and detrimental health directives. You’d recall that we had a discussion of the hoax behind the claim that humans need to consume very little saturated fats and salt, which heavily implicated Ancel Keys, who had the backing of the American Heart Association. Well, even in the status quo the American Heart Association recommends aiming for a dietary pattern that achieves less than 6% of total calories from saturated fat. This is to say, that for example, if you need about 2,000 calories a day, no more than 120 of them should come from saturated fat – the same saturated fat that has now been proven to be essential for your health and to play an essential role in the functionality of your body!

Well, this unaccountable attitude towards accurate nutritional science in the present (as well) is actually less surprising when you consider that the AHA has been operating as a corrupt, anti-health lobby institution for the medical industrial complex, and even food companies. For instance, this year, the American Heart Association sent an employee to TEXAS to fight a bill that would stop food stamps from covering unhealthy items such as candy and soda—part of the MAHA initiatives.

Well, when you follow the money, you understand why the AHA has these inclinations. Not only is it funded by many pharmaceutical corporations, but General Mills and Pepsi Co are both forum members of The American Heart Association.

The question then is, why have these associations averted scrutiny for all these years? Well, for one the people who back them, like the Rockefellers have deep pockets: they not only pay for their operations, but pay to insure they either receive positive coverage (think the mainstream media and vaccines), or pay to ensure they remain under the radar. The second reason is that these organisations play on the liberal inclinations of society, in a world where identity politics are also expected to govern organisational culture. For instance, (and this is not a joke), the American Medical Association declared WEIGHT measurement, through the Body Mass Index (or BMI) to be RACIST, of all things – which obviously fit well in a culture of “body positivity”, and negative reinforcement for unhealthy habits.

Written By Lindokuhle Mabaso

The medical industrial complex and scientistic cult evidently keep using the most vulnerable members of society (especially children) as a sacrifice in the pursuit of their efforts. But, with all that we know about the medical industrial complex, this is not news to anyone. In fact, what is expected is that there be progressive institutional reform in the status quo – especially in the second Trump administration – that directly challenges these issues. However, what is being exposed is just how deeply entrenched regulatory bodies are in their collusion with the medical industrial complex – especially pharmaceutical companies. But, today, we ought to discuss this further in light of Moderna’s mRNA COVID Shot getting Full FDA Approval for said to be “At-Risk” Infants.

U.S PRESIDENT DONALD TRUMP THREATENS 35% TARIFFS ON CANADA STARTING AUG. 1

U.S President Donald Trump has threatened a 35% tariff on goods imported from Canada. [ROLL CLIP00:11-] Trump’s announcement of higher tariffs on Canada comes amid a flurry of letters the U.S President has sent to world leaders over the past week informing them what rates their goods will be tariffed at come August 1, absent any trade deals.

BRAZIL VOWS RETALIATORY TARIFFS AGAINST US IF TRUMP FOLLOWS THROUGH ON 50% IMPORT TAXES

In a related matter, Brazilian President Luiz Inácio Lula da Silva has said that he will impose retaliatory tariffs on the United States if President Donald Trump follows through on a pledge to boost import taxes by 50% over the South American country’s criminal trial against his predecessor, Jair Bolsonaro. Lula said he will trigger Brazil’s reciprocity law approved by Congress earlier this year if negotiations with the U.S. fail.

NETANYAHU SAYS HOPING HOSTAGE DEAL WILL BE FINALIZED ‘IN A FEW DAYS’

On the last day of his 4-day trip to the US, Benjamin Netanyahu released a brief clip detailing his discussions with US President Donald Trump as well as Israel’s plans for Gaza amid ceasefire talks. Netanyahu emphasised Israel’s previous goals in Gaza including the removal of Hamas, demilitarisation of Gaza.

UK, FRANCE ANNOUNCE AGREEMENT ON PILOT MIGRANT RETURNS PROGRAM

British Prime Minister Keir Starmer and French President Emmanuel Macron have reached an agreement on a pilot programme to return migrants and refugees arriving in small boats, in a scheme to curb crossings over the English Channel. In a joint press conference on Thursday, Starmer said people arriving in the United Kingdom on small boats will “be detained and returned to France in short order”.

MODERNA’S mRNA COVID SHOT GETS FULL FDA APPROVAL FOR “AT-RISK” INFANTS

On July 10, 2025, the FDA granted full approval for Moderna’s mRNA COVID-19 vaccine (Spikevax) in “at-risk” children aged 6 months to 11 years. The shot was previously available only under emergency use authorization. This approval comes despite a mountain of evidence linking the shots to catastrophic harms, some of which include heart damage, brain damage, cancer, and mass death. Once again, this decision is quite concerning as it shows that regulatory agencies remain captured by the Bio-Pharmaceutical Complex. And so, one has to ask: How many more children must be sacrificed before accountability begins?

THIS MOVE COMPOUNDS THE LACK OF TRUST TOWARDS THE FDA

Now, this move certainly compounds the lack of trust towards the FDA, and necessarily so when you consider who influences the policy direction of the FDA. The general points of historical context to note regarding the FDA is that it was established in 1906 in response to public concern over unsafe food and drugs, such as spoiled food and counterfeit products. However, food industry lobbyists gradually gained influence, leading to the removal of the agency’s original leader. As a result, numerous harmful food additives were granted “generally recognised as safe” (GRAS) status and continue to be used today.

Then, in 1962, the FDA was given broad powers to oversee drug safety following the thalidomide incident. Unfortunately, the new regulations created strict standards for drug efficacy that were often selectively enforced, benefiting the pharmaceutical industry. Unfortunately, the FDA then increasingly targeted natural therapies, which led to many being erased from history – all of which is incredibly important to remember in light of our subsequent discussion on the propaganda against salt. Nevertheless, this historical context is why – despite the numerous attempts to reform the agency – issues of inefficiency and bias within the FDA persist. [PAUSE]

Now, evidence of the lobbyist factor in the FDA’s work, can be inferred in the agency’s work in food regulation. For instance, in the late 1800s, food producers were selling adulterated products, and pharmaceutical companies peddled medicines with secret ingredients like opium and alcohol. Public outrage grew, especially after exposés like Upton Sinclair’s ‘The Jungle’, which helped spark the 1906 Pure Food and Drug Act. This law gave the Bureau of Chemistry the power to ensure accurate labeling and prevent harmful additives in food.

Well, the director of the Bureau of Chemistry (and thus the first head of the FDA), Harvey Wiley conducted tests on food additives, proving they made healthy volunteers sick. While the public and many scientists supported his findings, the food industry fought back with powerful lobbyists and legal tactics. Well, Wiley’s book “The History of A Crime Against The Food Law” went on to detail much of the same abhorrent industry tactics we see happening now. But, this is all to detail the contextual background behind the FDA’s propensity to be influenced by lobbyists from the industries it is supposed to regulate – which is the first aspect of the FDA’s problem with corruption.

THE FDA’S DECEPTIVE AND HARMFUL “GENERALLY RECOGNISED AS SAFE” STATUS

Let’s then proceed to discuss the FDA’s “Generally Recognised as Safe” status. Many food additives are “generally recognised as safe” (or GRAS), and what this actually means is that they are widely used but WITHOUT REGULATION! Well, GRAS food products presented two fundamental issues: food industry counterfeiting and harmful additives. More specifically, the industry often fakes products to cut costs; for instance honey is often faked by adding cheap syrups or other ingredients to mimic its appearance and taste; while polluted waters are also added to enlarge oysters.

Now, despite evidence of harm, the food industry claimed these additives were essential for production, even though competitors showed higher-quality (and ultimately more profitable) products could be made without them. However, there were warnings that chronic exposure to additives could cause long-term health issues, such as organ damage; and these warnings were ignored – especially as the influence of industry lobbyists grew – which is why these harmful additives and faked foods were eventually reclassified as “generally recognized as safe.” But of course, these so-called “safe” additives have contributed to widespread chronic illness in society. Here’s more on the FDA’s GRAS status.

Furthermore, companies currently self-certify their chemicals without independent oversight; which has resulted in ingredients like titanium dioxide – which is banned in Europe and other developed nations still being legal in the US despite mounting health concerns. Through GRAS, FDA has for the longest time applied an “innocent until proven guilty” approach to food! Which is a categorically dangerous approach; ingredients should not have to harm or kill people first before they are deemed unsafe!

PETER MARKS AND THE FDA’S COVER-UP OF THE HARMS OF COVID JABS

Let’s also look at vaccine cover-ups, as being part of the reasons behind the compounding lack of trust towards the FDA. Many have been horrified to learn that the FDA and CDC systematically ignored every possible sign the COVID vaccines were dangerous as they pushed it on more and more people. One of the ways people were made aware of this was through the recently leaked recordings showing how stubbornly the head of FDA’s vaccine division, being Peter Marks at the time, refused to acknowledge any of the evidence brought forward by a group of permanently injured vaccine recipients, and even medical practitioners who were treating vaccine injured patients.

Here’s why this is important to note: generally, in looking through what transpired with the COVID-19 response, Anthony Fauci is commonly blamed for all that went amiss – and correctly so. However, we must not also miss the people who were also directly involved, while hidden within the FDA bureaucracy. One such person is Peter Marks. Peter Marks is the primary person who covered up the reports of COVID vaccine injuries (and instead repeatedly told the world they were (quote unquote) “safe and effective”). He was also the person who kept on pushing the FDA’s chief vaccine scientists (who were very pro-vaccine) to accelerate and condense the approval timelines for the COVID jabs (as those approvals were needed to legally implement Biden’s vaccine and booster mandates). The parties involved in this process, which included, Marion Gruber and Philip Krause (who were the Director and Deputy Director of the FDA’s Office of Vaccines Research and Review, respectively); they reported that there were (at that point) no more corners they could cut to further accelerate the COVID vaccine approvals, at which point they were removed from the COVID vaccine approval process and Peter Marks took it over (at which point the unjustifiable approvals and mandates quickly followed).

THE PROBLEMS WITH THE FDA ARE FURTHER ENABLES BY STANDARDS IN MEDICINE

So, while the FDA is central to focus on as far as recent developments are concerned, it’s important also to note that the problems with the FDA are FURTHER enabled by standards in medicine. And I say that because it occurred to me that even if we have bad regulators who approve bad medicine, if we had good doctors and medical standards, then the harms could easily be averted or mitigated. But if the medical standard is overmedication and trusting “the science”, while doctors function as pharmaceutical representatives, then of course the problems are worse.

Let’s look at medical education. No matter how you dice it, medical education is quite challenging as there is simply too much to learn, and so even the “brightest” students adopt a triage mentality where they cut out things that NOTt necessary (or low-yield) (specifically) for exams so they can pass and get a degree. And because of this medical education typically presents 3 issues as far as medical standards are concerned.

First, the present standard of medical education covers many aspects in a superficial manner (e.g., med students just learn the classic indications, simple mechanisms of action and commonly recognized side effects of drugs). Now, this is quite problematic as many of those simplistic facts students memorize aren’t always entirely correct (or become evidently contradictory once you take the time to understand them). However, since students are under such pressure to memorize them, they take the facts as verbatim facts they don’t question and become quite haughty towards those who do.

Second, there has been a strong focus in medicine on the key medical products on the market (e.g., doctors focus on how to use pharmaceutical drugs along with the key microbes and their pharmaceutical treatments, understanding what aspects of the body each speciality is responsible for, how to interpret imaging studies, and even how to understand surgery well enough to want to go into it or refer patients to it). Similarly, there is also a strong focus on just the basic skills necessary for being a doctor (this includes being able to recognize potentially life-threatening conditions, conducting a physical exam with enough details to complete a medical note and writing billable medical notes). That said, there is also (thankfully) a strong focus on anatomy and physiology, which along with recognising key diseases and medical emergencies, represent some of the most valuable aspects of conventional medical training.

Then the third issue presented as far as medical standards are concerned has to do with how medical training cuts out a lot of the subtle aspects of medical science and doctoring that make you an effective clinician (and this includes things like medical ethics). And because of this, there is always a subset of medical students who have that inherent capacity and excel at being clinicians but very few learn it through their training. Put differently, standard medical training does NOT really cover what is needed to make people healthy as there is never enough time for that and again and again, we hear stories of medical educators who try to incorporate it but get pushed to the side due to limited curriculum time.

So, in a world where medical standards prioritise pharmaceutical interventions, and medical education and training focuses purely on passing exams as opposed to being more concerned with aspects of medical science that make a med student an effective clinician, well then of course the FDA’s corruption will have crippling impact, because doctors themselves are trained to push what the FDA has approved.

Well, no wonder the medical industrial complex is so-multilayered. There are clearly various actors involved. But, this also gives broader context behind why doctors become progressively less focused at making their patients better, while becoming product pushers for the pharmaceutical industry. Take this testimony from a pharmaceutical representative of 32 years. She exposes the corrupt relationship between big pharma and doctors, primarily based on greed because it was about organising expensive gifts and experiences for doctors in exchange for their product loyalty.

WORST OF ALL IS THAT PATIENTS ARE DISADVANTAGED BY THE MEDICAL SYSTEMS

I’ve had discussions with medical students and practitioners on the necessity of strict standards to enter medicine because it is one of those fields where there is no room for error. ANd I think many people still have that same perception of the medical field: which is that it brings in the best and trains them rigorously so they are less susceptible to making mistakes that can be the difference between life and death for some. BUT… while there absolutely are exceptions who are incredible doctors, it is also clear that the medical system is not as fool, corruption, and greed-proof as we thought. And worse of all is that there are many people who have not broken free from this presumption of excellence and efficacy in the medical field, and pay with their lives. And yet, the issues in medicine are quite nuanced because it is NOT just the FDA that has been financially bought out – it is almost everyone, down to the medical schools that teach the doctors that are supposed to practise evidence based and holistic medicine. In fact, the verdict from good doctors is that there is almost no such thing as evidence-based medicine anymore, in a world where big pharma has gained influence over regulators and academia.

Written By Lindokuhle Mabaso

The court found that the Commission failed to comply with transparency obligations, particularly concerning the negotiation and content of vaccine deals made during the height of the pandemic. This includes contracts signed with major pharmaceutical companies like Pfizer and Moderna.

Critics have long accused the Commission of a lack of accountability, especially regarding reported personal text communications between von der Leyen and Pfizer CEO Albert Bourla. These texts were allegedly used to negotiate key terms of the vaccine contracts, but were never disclosed despite formal requests from journalists and Members of the European Parliament.

The ECJ’s ruling states that the failure to provide access to those communications constitutes a breach of EU transparency laws.

Von der Leyen and the Commission have not yet responded to the ruling. However, legal experts suggest the judgment may open the door to further legal and political scrutiny over the EU’s pandemic response and the billions of euros spent on vaccine procurement.